跳至主要内容
临床试验/NCT00857922
NCT00857922招募中不适用

Neurosciences Research Repository

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 15,000 人开始时间: 2009年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
15,000
试验地点
2
主要终点
Discharge status

研究概览

简要总结

In order to expand neuroscience research and move laboratory advances to patients, there is a need to integrate reliable clinical data with biologic information from patient tissue specimens. The Neuroscience Research Repository (NRR) seeks to meet this need. The NRR is a prospective database and sample bank created to collect information and samples for current and future neuroscience research. The objective of this NRR is to develop a data and sample repository for study of neurological conditions. A repository utilizing standardized electronic health data and samples collected in a uniform manner serves to foster the ability to perform research on current and future projects. Samples and data for clinical, genomic and proteomic analysis will be provided to optimize their value for neuroscience research.

The NRR will enroll patients and collect clinically recorded longitudinal data for as long as they are followed by the Neurosurgery service and up to an additional 5 years after being released from care. Patients will be enrolled on admission to the service and samples will be taken at three time points: Time One, within 24 hours of event (preferably first blood draw); Time Two, within 48 hours of event; and Time Three, time of any residual tissue availability. Family members of select groups of patients will also be approached for enrollment.

Samples and data will be labeled with a study code to maintain confidentiality. Samples and data will be maintained in secure, limited access environments with back-up/redundancy procedures in place. Sample inventory will be maintained with a bar-coding system. A duty to warn clause will be included in the consent as will the determination of willingness to be re-contacted for future research. Time of sample acquisition to time of sample processing will be documented for quality control purposes. Freezers will be monitored for temperature stability. Recipient investigators will be requested to provide feedback on sample quality. Samples will be distributed to neuroscience investigators after approval from the Neurosurgery Scientific Review Committee - Dissemination Review Committee and the Committee for the Protection of Human Subjects (CPHS).

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
0 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Neurosurgical patient (primary or consulting); patients<18 includes residual tissue only, no blood samples.
  • Family members of specific vascular, trauma, brain tumor and functional disorder cohorts (will be identified in future addendums to this repository)

排除标准

  • 1. Inability to obtain informed consent

研究组 & 干预措施

Neurosurgical patient

Neurosurgical patient of the Mischer Neuroscience Institute, 18 years and over

干预措施: tissue and data repository (Other)

Family members

Family members of specific vascular, trauma, brain tumor and functional disorder cohorts

干预措施: tissue and data repository (Other)

结局指标

主要结局

Discharge status

时间窗: hospital discharge

Standardized functional outcome score

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Georgene Hergenroeder

Study Director, PI, Associate Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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